ジャーナル論文 Reproducible Chiroptical Activity from Aggregated Chiral Thienopyrroledione–Fluorene π‑Conjugated Polymers.
Nao Suzuki (author) (この著者で検索)
University of Tsukuba a Institute of Pure and Applied Sciences
;
Ziwei Hu (author) (この著者で検索)
;
Sota Nakayama (author) (この著者で検索)
;
Soh Kushida (author) (この著者で検索)
;
Yohei Yamamoto (author) (この著者で検索)
;
Wijak Yospanya (author) (この著者で検索)
;
Reiko Oda (author) (この著者で検索)
;
Takaki Kanbara (author) (この著者で検索)
;
Junpei Kuwabara (author) (この著者で検索)
コレクション

引用
Nao Suzuki, Ziwei Hu, Sota Nakayama, Soh Kushida, Yohei Yamamoto, Wijak Yospanya, Reiko Oda, Takaki Kanbara, Junpei Kuwabara. Reproducible Chiroptical Activity from Aggregated Chiral Thienopyrroledione–Fluorene π‑Conjugated Polymers.. Science and Technology of Advanced Materials. 2026, 27 (), 2680968 . https://doi.org/10.1080/14686996.2026.2680968

説明:

(abstract)

Chiral π‑conjugated polymers have attracted considerable interest because their chiral aggregated structures can generate pronounced chiroptical responses. Here, we report the design, synthesis, and chiroptical characterization of fluorene – thienopyrroledione polymers bearing a single chiral center in each repeating unit, (R)- and (S)-PFTPD, prepared via direct arylation polycondensation to minimize structural defects. Although only weak chiroptical activity was observed in a solution, addition of 1‑butanol to CHCl3 solutions of the polymers induced the formation of stable aggregates that exhibited strong circular dichroism (CD) and circularly polarized luminescence (CPL). Systematic examination of the sample preparation parameters revealed that the mixing process critically influences the chiroptical properties. Dropwise addition of 1-butanol under controlled stirring provided the most reliable results, yielding highly reproducible CD spectra. Under these optimized conditions, the aggregates exhibited an average dissymmetry factor (|gabs|) of 1.5 × 10−2 and a CPL dissymmetry factor (|glum|) of 1.9 × 10−2. These values rank among the highest reported for π-conjugated polymer aggregates bearing only a single chiral source per repeat unit. This study demonstrates that precise control over the solvent-mixing process is essential for the reproducible emergence of chiroptical properties and highlights the chiral TPD unit as a promising platform for chiroptical polymer materials.

権利情報:

キーワード: Chiral π‑conjugated polymer, thienopyrroledione, circular dichroism, circularly polarized luminescence

刊行年月日: 2026-06-02

出版者: National Institute for Materials Science

掲載誌:

  • Science and Technology of Advanced Materials (ISSN: 14686996) vol. 27 2680968

研究助成金:

原稿種別: 著者最終稿 (Accepted manuscript)

MDR DOI: https://doi.org/10.48505/nims.6345

公開URL: https://doi.org/10.1080/14686996.2026.2680968

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更新時刻: 2026-06-19 13:05:19 +0900

MDRでの公開時刻: 2026-06-19 14:29:50 +0900

ファイル名 サイズ
ファイル名 Reproducible chiroptical activity from aggregated chiral thienopyrroledione fluorene conjugated polymers.pdf (サムネイル)
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ファイル名 Revised_SI.pdf
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ファイル名 STAM-2026-0104_data.zip
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